Canonical Allele Identifier: CA9640271

Gene: PRKCG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889743T>A , CM000681.2:g.53889743T>A	GRCh38
NC_000019.9:g.54392997T>A , CM000681.1:g.54392997T>A	GRCh37
NC_000019.8:g.59084809T>A	NCBI36
NG_009114.1:g.12531T>A , LRG_669:g.12531T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.391T>A	ENSP00000507230.1:p.Cys131Ser
ENST00000682268.1:n.689T>A
ENST00000682902.1:n.693T>A
ENST00000683513.1:c.391T>A	ENSP00000506809.1:p.Cys131Ser
ENST00000263431.4:c.391T>A MANE Select	ENSP00000263431.3:p.Cys131Ser
ENST00000263431.3:c.391T>A	ENSP00000263431.3:p.Cys131Ser
ENST00000419486.1:c.7T>A	ENSP00000387919.2:p.Cys3Ser
ENST00000474397.5:c.7T>A	ENSP00000471271.1:p.Cys3Ser
ENST00000479081.5:c.7T>A	ENSP00000471544.1:p.Cys3Ser
NM_001316329.1:c.391T>A	NP_001303258.1:p.Cys131Ser
NM_002739.3:c.391T>A , LRG_669t1:c.391T>A	NP_002730.1:p.Cys131Ser
NM_002739.4:c.391T>A	NP_002730.1:p.Cys131Ser
NM_002739.5:c.391T>A MANE Select	NP_002730.1:p.Cys131Ser
NM_001316329.2:c.391T>A	NP_001303258.1:p.Cys131Ser